Received May 30, 2002
Accepted September 3, 2002
Molecular Mechanisms of Proline-Mediated Tolerance to Toxic Heavy Metals in Transgenic
Microalgae
Surasak Siripornadulsil 1, Samuel Traina 2, Desh Pal S. Verma 3, and Richard T. Sayre 4*
1
Biophysics Program, Ohio State University, Columbus, Ohio 43210
2
Department of Natural Resources, Ohio State University, Columbus, Ohio 43210
3
Department of Molecular Genetics and Plant Biotechnology Center, Ohio State University,
Columbus, Ohio 43210
4
Biophysics Program, Ohio State University, Columbus, Ohio 43210; Department
of Plant Biology and Biophysics Program, Ohio State University, Columbus, Ohio 43210
* To whom correspondence should be addressed. E-mail: sayre.2{at}osu.edu.
Pro has been shown to play an important role in ameliorating environmental stress
in plants and microorganisms, including heavy metal stress. Here, we describe the
effects of the expression of a mothbean
1-pyrroline-5-carboxylate
synthetase (P5CS) gene in the green microalga Chlamydomonas reinhardtii
. We show that transgenic algae expressing the mothbean P5CS gene have
80% higher free-Pro levels than wild-type cells, grow more rapidly in toxic Cd concentrations
(100 µM), and bind fourfold more Cd than wild-type cells. In addition, Cd-K edge
extended x-ray absorption fine structure studies indicated that Cd does not bind
to free Pro in transgenic algae with increased Pro levels but is coordinated tetrahedrally
by sulfur of phytochelatin. In contrast to P5CS-expressing cells, Cd is coordinated
tetrahedrally by two oxygen and two sulfur atoms in wild-type cells. Measurements
of reduced/oxidized GSH ratios and analyses of levels of malondialdehyde, a product
of the free radical damage of lipids, indicate that free Pro levels are correlated
with the GSH redox state and malondialdehyde levels in heavy metal-treated
algae. These results suggest that the free Pro likely acts as an antioxidant in Cd-stressed
cells. The resulting increased GSH levels facilitate increased phytochelatin synthesis
and sequestration of Cd, because GSH-heavy metal adducts are the substrates
for phytochelatin synthase.